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Doctors are prescribing spironolactone more often to treat acne and skin conditions in teenagers, and it seems safe and well-tolerated.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

People with chronic Alopecia Areata often have lower vitamin D levels.

Vitamin D receptor is essential for healthy bones and skin.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Hirsutism is excessive hair growth in women often caused by polycystic ovarian syndrome, and identifying the cause is important for managing associated health risks.

3α-AdiolG is a good marker for androgen activity in women with excessive hair growth and decreases with anti-androgen treatment.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Glucocorticoid and mineralocorticoid therapy effectively manage Congenital Adrenal Hyperplasia symptoms but have limitations.

Hormonal therapies, especially antiandrogens, can help manage Hidradenitis Suppurativa.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

A 73-year-old woman's unusual hair loss and growth led to the discovery of a rare condition causing too much testosterone, which improved after her ovaries were removed.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

PCOS should be reclassified into two types based on hormone levels and symptoms.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

Hirsutism, excessive hair growth in women, often caused by high androgen levels and polycystic ovary syndrome, can be treated with medication and weight management.

Finasteride effectively inhibits the enzyme steroid 5 alpha-reductase II.

New mutations in the hairless gene may cause hair loss and affect bone development.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

A 12-year-old girl with very high testosterone and insulin resistance improved with birth control pills, suggesting PCOS can cause high testosterone without tumors.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

RHUPUS should be considered in children with deforming arthritis.

A 17-year-old with Netherton syndrome has dry, itchy skin, brittle hair, and high IgE levels, treated with antihistamines and emollients.

A specific gene mutation causes a severe skin disorder in a family.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.